Canonical Allele Identifier: PA2827616874
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 913959
ClinVar RCV Id: RCV001167853 RCV001169725 RCV003336308
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Phe1756Tyr
CA375321398
NM_001351527.2:c.5267T>A